WO2018147251A1 - Thermally adhesive sheath-core conjugate fiber and tricot fabric - Google Patents
Thermally adhesive sheath-core conjugate fiber and tricot fabric Download PDFInfo
- Publication number
- WO2018147251A1 WO2018147251A1 PCT/JP2018/003927 JP2018003927W WO2018147251A1 WO 2018147251 A1 WO2018147251 A1 WO 2018147251A1 JP 2018003927 W JP2018003927 W JP 2018003927W WO 2018147251 A1 WO2018147251 A1 WO 2018147251A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- core
- sheath
- polyester
- melting point
- composite fiber
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Images
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/12—Stretch-spinning methods
- D01D5/16—Stretch-spinning methods using rollers, or like mechanical devices, e.g. snubbing pins
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/14—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyester as constituent
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/28—Formation of filaments, threads, or the like while mixing different spinning solutions or melts during the spinning operation; Spinnerette packs therefor
- D01D5/30—Conjugate filaments; Spinnerette packs therefor
- D01D5/34—Core-skin structure; Spinnerette packs therefor
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04B—KNITTING
- D04B21/00—Warp knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes
- D04B21/06—Patterned fabrics or articles
- D04B21/08—Patterned fabrics or articles characterised by thread material
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04B—KNITTING
- D04B21/00—Warp knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes
- D04B21/14—Fabrics characterised by the incorporation by knitting, in one or more thread, fleece, or fabric layers, of reinforcing, binding, or decorative threads; Fabrics incorporating small auxiliary elements, e.g. for decorative purposes
- D04B21/16—Fabrics characterised by the incorporation by knitting, in one or more thread, fleece, or fabric layers, of reinforcing, binding, or decorative threads; Fabrics incorporating small auxiliary elements, e.g. for decorative purposes incorporating synthetic threads
Definitions
- the present invention has less fuzz generation in high-order processes, is excellent in high-order passage even in applications with high quality requirements such as tricot use, and the woven or knitted fabric after heat bonding is excellent in strength, dimensional stability, and durability.
- the present invention relates to a heat-adhesive core-sheath composite fiber excellent in quality as a flow passage material for a liquid filtration membrane.
- Polyester fibers are suitable as raw materials for clothing, industrial materials, etc. due to their excellent dimensional stability, weather resistance, mechanical properties, durability, and productivity that can be mass-produced relatively inexpensively. Used in applications.
- polyester fiber having thermal adhesiveness a yarn composed of two or more kinds of polyesters having different melting points or softening points is suitable.
- mode for example, mixed yarn made of filament yarn, core-sheath type or side-by-side type composite fiber can be mentioned.
- a composite fiber composed of polymers having different melting points is superior in quality after thermal bonding.
- a core-sheath composite yarn excellent in quality such as productivity of raw yarn and surface smoothness of the fabric after heat treatment
- the sheath component is composed of a component having a melting point or a softening point lower than that of the core component.
- Sheath-type composite fibers are actively used.
- a core-sheath type composite fiber having a polyester whose main repeating unit is ethylene terephthalate as a core part and a polymer having a softening temperature of 130 to 200 ° C. as a sheath part has been proposed.
- the core-sheath-type conjugate fiber it has a predetermined strength and elongation characteristic, does not cause misalignment due to displacement at the thermal bonding intersection, and does not generate wrinkles. Is done.
- the polymer in the sheath portion has a low crystallinity having no clear melting point, as exemplified by polyester copolymerized with isophthalic acid. For this reason, when the woven or knitted fabric made of the core-sheath type composite fiber is heat-bonded, unevenness occurs in the bonding between the composite fibers, resulting in dimensional stability, variation in the strength and elongation of the fabric, and the like. There was a problem of poor quality when used as a material.
- Patent Document 2 a core-sheath type composite fiber in which 90 mol% or more of repeating units have a core made of a polymer composed of ethylene terephthalate and 60 to 90 mol% of repeating units have a copolymer polybutylene terephthalate made of butylene terephthalate as a sheath.
- Patent Document 2 a core-sheath type composite fiber in which 90 mol% or more of repeating units have a core made of a polymer composed of ethylene terephthalate and 60 to 90 mol% of repeating units have a copolymer polybutylene terephthalate made of butylene terephthalate as a sheath.
- the sheath component is imparted with appropriate crystallinity, and since the fiber physical properties such as the boiling water shrinkage rate and the peak temperature of the heat shrinkage stress are good, the heat of good quality. It is said that a bonded knitted or knitted product can be obtained.
- the present invention eliminates the problems of the prior art, has less fuzz generation in high-order processes, is excellent in high-order passage even in applications with high quality requirements such as tricot use, and the woven or knitted fabric after heat bonding has strength, dimensions Provided is a heat-adhesive core-sheath composite fiber that is excellent in stability and durability and excellent in quality as a flow passage material for a liquid filtration membrane.
- a core-sheath type composite fiber having a polyester having a melting point of 250 ° C. or higher as a core, a melting point of 215 ° C. or higher and a polyester having a melting point 20 to 35 ° C. lower than that of the polyester constituting the core.
- the present invention there is little fluffing in a high-order process, excellent high-order passability even in applications with high quality requirements such as tricot use, and the woven or knitted fabric after heat bonding has strength, dimensional stability, and durability. It is possible to provide a heat-bondable core-sheath composite fiber that is excellent and excellent in quality as a flow passage material for a liquid filtration membrane.
- FIG. 1 shows an example of a single yarn cross-sectional shape of a heat-adhesive core-sheath composite fiber preferably used in the present invention.
- FIG. 2 is an example of a single yarn cross-sectional shape of the thermoadhesive core-sheath conjugate fiber of the present invention, and is a view for explaining the cross-sectional eccentricity.
- the core-sheath type composite fiber of the present invention is composed of a polyester having a melting point of the core component of 250 ° C. or higher, a polyester having a melting point of 215 ° C. or higher, and 20 to 35 ° C. lower than the melting point of the polyester constituting the core.
- the spinning temperature can be increased to such an extent that the strength and elongation characteristics of the polyester can be maximized, and the strength and durability when used as a fabric are excellent.
- the melting point of the core component polyester is preferably 270 ° C. or less from the practical upper limit. It is preferable that the melting point of the core component polyester is 270 ° C. or lower because it is not necessary to perform spinning at an extremely high temperature and spinning can be performed using a general-purpose melt spinning apparatus. More preferably, it is 253 degreeC or more and 260 degrees C or less.
- the melting point of the sheath component polyester is 215 ° C or higher, preferably 250 ° C or lower. It is preferable that the melting point of the sheath component polyester is 250 ° C. or lower because a general-purpose apparatus can be used when the fabric is thermally bonded, and fuming caused by the oil component in the thermal bonding treatment can be suppressed. More preferably, it is 220 degreeC or more and 235 degreeC or less.
- the thermal bonding temperature of the fabric can be made sufficiently lower than the melting point of the core component polyester, It can be a durable fabric. Further, by setting the difference in melting point to 35 ° C.
- the spinning temperature can be set to a temperature that maximizes the strength of the core component polyester and suppresses the thermal degradation of the sheath component polyester as much as possible. This is a composite fiber that is superior in quality and excellent in quality with little raw yarn fluff.
- the difference in melting point between the sheath component polyester and the core component polyester is preferably 23 ° C. or higher and 30 ° C. or lower.
- the softening temperature of the core component polyester is preferably 245 ° C. or higher, and the softening temperature of the sheath component polyester is preferably 205 ° C. or higher. It is preferable that the softening temperature of the core component polyester is 245 ° C. or higher because when the fabric is heat-bonded at the melting point or higher of the sheath component polyester, the dimensional change is small and the fabric form is stable.
- the softening temperature of the core component polyester is more preferably 250 ° C. or higher.
- the upper limit temperature of the softening temperature of the core component polyester is practically 270 ° C.
- the softening temperature of the sheath component polyester is 205 ° C. or higher because there is no fusion to the heater during heat setting in the processing step, and the high-speed passage is stable.
- the softening temperature of the sheath component polyester is more preferably 215 ° C. or higher.
- any polyester can be selected as long as the melting point is within the above range, but polyethylene terephthalate (hereinafter referred to as PET) is preferable from the viewpoint of dimensional stability and strong elongation characteristics.
- PET is a polyester obtained using terephthalic acid as the main acid component and ethylene glycol as the main glycol component.
- the core component polyester may appropriately include a copolymer component as long as the melting point is within the above-described range.
- Examples of the copolymerizable compound include PET, dicarboxylic acids such as isophthalic acid, succinic acid, cyclohexanedicarboxylic acid, adipic acid, dimer acid, sebacic acid, 5-sodium sulfoisophthalic acid, ethylene glycol, diethylene glycol, 2 , 2-dimethyl-1,3-propanediol, butanediol, neopentyl glycol, cyclohexanedimethanol, polyethylene glycol, polypropylene glycol, bisphenol A ethylene oxide adduct, and the like.
- dicarboxylic acids such as isophthalic acid, succinic acid, cyclohexanedicarboxylic acid, adipic acid, dimer acid, sebacic acid, 5-sodium sulfoisophthalic acid, ethylene glycol, diethylene glycol, 2 , 2-dimethyl-1,3-propanediol
- the PET is a homo-PET comprising 100% repeating units of ethylene terephthalate. If necessary, inorganic fine particles such as titanium dioxide as a matting agent and silica fine particles as a lubricant may be added.
- any polyester can be selected as long as the melting point is within the above-mentioned range, but in addition to PET, polytrimethylene terephthalate and polybutylene terephthalate are preferable.
- PET polytrimethylene terephthalate
- PET polybutylene terephthalate
- an arbitrary copolymer component can be added at an arbitrary ratio as long as the melting point is within the above-mentioned range.
- the copolymer PET is composed of 70% by mole or more of ethylene terephthalate repeating units, Moderate crystallinity can be imparted, and spinning operability is stabilized.
- a copolymerized PET composed of ethylene terephthalate repeating units. Even when a polymer other than PET is used as the sheath component polyester, a copolymer component can be appropriately added within a range that does not impair the raw yarn productivity and the quality of the fabric after the thermal bonding treatment.
- a copolymerization component arbitrary components, such as the above-mentioned copolymerization component, can be copolymerized.
- inorganic fine particles such as titanium dioxide as a matting agent and silica fine particles as a lubricant may be added as needed, regardless of the polymer species selected.
- the intrinsic viscosity (hereinafter referred to as IV) of the composite fiber is preferably 0.55 to 0.75.
- IV the intrinsic viscosity
- the IV is 0.55 or more, the degree of polymerization is not too low, and it is preferable because the toughness sufficient for the composite fiber to withstand practical use can be achieved.
- the IV is 0.75 or less, the IV is not too high at the time of spinning, there is no need to perform extreme high temperature spinning, the increase in the amount of COOH during melt spinning can be suppressed, and melt fracture may occur. This is preferable because a uniform composite fiber is obtained and the toughness is not lowered. More preferably, IV is in the range of 0.60 to 0.70.
- FIG. 1 is a schematic cross-sectional view of a core-sheath type composite fiber of the present invention, which shows a core-sheath type composite fiber 10 in which a core component 1 is surrounded by a sheath component 2.
- the cross-sectional shape of the composite fiber is not particularly limited as long as the high melting point component is disposed in the core portion and the low melting point component is disposed in the sheath shape covering the core portion, but the sheath component completely covers the core component, and the core component It is preferable that there is no exposure.
- the eccentricity of the center of gravity of the core component with respect to the center of gravity of the entire composite fiber is preferably 5% or less in the cross section of the composite fiber.
- An eccentricity of 5% or less is preferable because a coil-like crimp does not appear even if the combination of the core component and the sheath component is a combination that causes a shrinkage difference, and the fabric quality is excellent. More preferably, the eccentricity is 1% or less.
- the cross-sectional outer peripheral shape of the composite fiber is preferably a substantially circular shape having a flatness expressed by A / B of 1.1 or less, where A is the major axis and B is the minor axis.
- A is the major axis
- B is the minor axis.
- the content of the inorganic particles contained in the core component is preferably 3.0% by weight or less because the toughness is improved, and more preferably 0.5% by weight or less.
- the content of the inorganic fine particles contained in the sheath component is preferably 0.05% by weight or more because process passability is improved. More preferably, the content of the inorganic fine particles contained in the sheath component is 0.05% by weight or more and 0.5% by weight or less without excessive wear of the guide during the process, when used as a flow path material, It is preferable because unnecessary inorganic particles are not dropped off.
- the inorganic fine particles are preferably titanium oxide from the viewpoint of process passability as a composite fiber.
- the total fineness is preferably 30 dtex or more. By setting the total fineness to 30 dtex or more, sufficient strength and rigidity can be ensured even by heat bonding treatment, and when used as a flow path material, a sufficient amount of permeate flows even if water pressure acts. Can be secured.
- the total fineness is preferably 90 dtex or less, more preferably 40 dtex or more. By setting the total fineness to 90 dtex or less, the fabric can be thinned, and when used as a flow path material, the number of layers per unit formed by bonding the filtration membrane and the flow path material can be increased.
- the single yarn fineness of the composite fiber is preferably 3.0 dtex or less.
- the single yarn fineness is preferably 0.7 dtex or more, and more preferably 1.5 dtex or more and 2.5 dtex or less. By setting the single yarn fineness to 0.7 dtex or more, there is little yarn unevenness and raw yarn fluff, and stable yarn production is possible. It is preferable because an appropriate rigidity can be obtained.
- the strength of the composite fiber is 3.8 cN / dtex or more, and the elongation is 35% or more.
- the strength is high when used as a fabric, and the durability when used as a flow path material is excellent.
- the practical upper limit is a strength of 7.0 cN / dtex.
- the elongation is 35 to 50%. A woven or knitted fabric obtained by setting the elongation to 50% or less is preferable because of excellent dimensional stability.
- the Worcester unevenness U% which is an index of thickness unevenness in the fiber longitudinal direction of the composite fiber, is 1.4% or less.
- Wooster spots U% of 1.4% or less is preferable because the surface of the fabric after thermal bonding becomes smooth and a uniform channel can be formed when used as a channel material. More preferably, the Wooster plaque U% is 1.0% or less.
- the dry heat shrinkage of the composite fiber is preferably 20% or less. It is preferable to set the dry heat shrinkage rate to 20% or less because dimensional changes due to thermal bonding treatment can be suppressed.
- the practical lower limit is a dry heat shrinkage of 2.0%.
- a preferred yarn production method for achieving the object of the present invention will be described.
- the die used for the melt spinning method of the heat-adhesive core-sheath composite fiber of the present invention an existing composite spinning die can be used.
- Examples of the melting method include a method using a pressure melter and a method using an extruder, but melting using an extruder is preferable from the viewpoint of efficiency and suppression of decomposition.
- the melting temperature is preferably set to 10 to 40 ° C. higher than the melting point of the polymer used.
- a preferable spinning temperature is 280 to 295 ° C. More preferably, the spinning temperature is 285 ° C to 293 ° C. By adopting such a spinning temperature, it is possible to obtain a composite fiber having high toughness and good spinning properties.
- a heater may be provided under the base.
- both the core component and sheath component are melted and kneaded separately, precisely discharged and weighed through a heating zone, passed through a filtration layer supplemented with foreign matter, and discharged and formed into a core and sheath using a composite die. ⁇ Cooled.
- the polymer residence time which is the transit time from melting to ejection, is within 30 minutes, thermal degradation of the polymer can be reduced, IV reduction can be suppressed, and yarn toughness reduction can be prevented.
- the polymer residence time is 20 minutes or less.
- the die surface temperature is preferably 270 ° C. or higher and 290 ° C. or lower.
- the base surface temperature is preferably 270 ° C. or higher, the core component characteristics can be maximized, and a yarn excellent in high elongation can be obtained.
- the die surface temperature is preferably 290 ° C. or less, an increase in yarn breakage due to deposition of polymer hydrolyzate directly under the die is suppressed, and this is preferable because it is excellent in raw yarn productivity.
- the core-sheath type composite fiber of the present invention is not only a two-step method in which the discharged polymer is once wound up as an undrawn yarn and then drawn, as well as a direct spinning drawing method or a high-speed spinning method in which spinning and drawing steps are continuously performed. It can be produced by any one-step method.
- the stretching temperature is preferably 60 ° C. or higher and 100 ° C. or lower, which is near the glass transition temperature of the undrawn yarn. Uniform stretching can be achieved by setting the stretching temperature to 60 ° C. or higher, and productivity deterioration due to fusion to a stretching roll or spontaneous elongation of fibers can be prevented by setting the stretching temperature to 100 ° C. or lower. More preferably, the stretching temperature is 75 ° C. or higher and 95 ° C. or lower.
- heat-set at a temperature at which the crystal speed of the undrawn yarn is maximized, and it is preferably set to 110 ° C. or higher and 180 ° C. or lower.
- Heat setting at 110 ° C. or higher is preferable because it can not only promote fiber crystallization and increase strength, but also stabilize various yarn properties such as shrinkage stress and dry heat shrinkage.
- Intrinsic viscosity (IV) ⁇ r of the definition formula is obtained by dissolving 0.8 g of a sample in 10 mL of O-chlorophenol (OCP) having a purity of 98% or more, and obtaining the relative viscosity ⁇ r using an Ostwald viscometer at a temperature of 25 ° C. according to the following formula: Intrinsic viscosity (IV) was calculated.
- OCP O-chlorophenol
- IV 0.0242 ⁇ r + 0.2634 [ ⁇ : viscosity of polymer solution, ⁇ 0: OCP viscosity, t: solution drop time (second), d: solution density (g / cm 3 ), t0: OCP drop time (second), d0: OCP Density (g / cm 3 )].
- the amount of permeated liquid after 5 days was measured, and the amount of fresh water produced per day was calculated. Based on the results of the test, the following evaluation points were used. 3 points: Magnesium sulfate salt removal rate of 99.8% or more and water production amount of 45 m 3 / day or more 2 points: Magnesium sulfate salt removal rate of 99.8% or more and water production amount of 40 m 3 / day or more of 45 m 3 / Day or the removal rate of magnesium sulfate salt is 99.0% or more and less than 99.8% and the amount of water produced is 45 m 3 / day or more 1 point: The removal rate of magnesium sulfate salt is 99.0% or more and 99.8% %, And the amount of water produced is 40 m 3 / day or more and less than 45 m 3 / day 0 point: The removal rate of magnesium sulfate salt is less than 99.0%, or the amount of water produced is less than 40 m 3 / day.
- Example 1 A homo-PET polymer of IV0.67 containing no titanium oxide (high melting point component, melting point 255 ° C.) and isophthalic acid and bisphenol A ethylene oxide adduct as the copolymer component are each 7.1 mol% based on the total acid component, A copolymerized PET polymer (low melting point component, melting point 230 ° C.) having a titanium oxide content of 0.05 wt% and IV 0.65 copolymerized with 4.4 mol% was prepared, and the high melting point component was 285 ° C. with an extruder.
- the low melting point component was melted at 260 ° C with an extruder, the spinning temperature was set at 290 ° C, weighed with a metering pump, filtered in a pack, and then with a nozzle nozzle as shown in FIG. It was discharged into a core-sheath composite type having a composite area ratio of 65:35 so that the cross-sectional shape of the concentric circular core-sheath was as follows (the cross-sectional eccentricity was 0% and the cross-sectional flatness was 1.0). At this time, it arrange
- a direct spinning method (DSD) is used which is consistently performed from drawing to winding, and the discharged polymer is set at a speed of 1728 m / min and a surface temperature of 85 ° C. through the cooling part and the oiling part. Then, the film was taken up by a take-up roll (first HR) and continuously drawn up to a heat treatment roll (second HR) set to 128 ° C. at 4489 m / min without being wound up, and stretched 2.6 times.
- first HR take-up roll
- second HR heat treatment roll
- the tension of the stretched and heat-treated yarns is adjusted with godet rollers (3rd GR and 4GR) set to speeds of 4549 m / min and 4584 m / min, respectively, and the tension is 0.20 cN / dtex at a speed of 4500 m / min.
- the cheese-like package was wound up to obtain a core-sheath type composite fiber of 56 dtex-24 filaments.
- the evaluation results for the obtained fibers are shown in Table 1.
- the Wooster spot U% was 0.4%
- the boiling water shrinkage was 10.3%
- the dry heat shrinkage was 17.2%.
- Examples 2 to 4 and Comparative Examples 1 to 3 In Examples 2 to 4 and Comparative Examples 1 to 3, the melting points of the core component polyester and the sheath component polyester were changed using the copolymer components used in the sheath component of Example 1, respectively. In accordance with Example 1, except that an appropriate spinning temperature was adopted. The evaluation results are shown in Table 1.
- Example 5 was the same as Example 1 except that the spinning machine was changed from DSD to the two-step method and the spinning conditions were adjusted accordingly. The evaluation results are shown in Table 1.
- Examples 6-7 Examples 6 to 7 were the same as Example 1 except that the shape of the discharge hole of the base was changed and the cross-sectional shape and the eccentricity of the core sheath were changed as shown in Table 2. The evaluation results are shown in Table 2.
- Examples 8-11 Examples 8 to 11 were the same as Example 1 except that the fineness of the composite fiber and the number of filaments were changed as shown in Table 2. The evaluation results are shown in Table 2.
- Examples 12-14 Example 12 to 14 were the same as Example 1 except that the amount of titanium oxide added to the core component polyester and the sheath component polyester was changed as shown in Table 3. The evaluation results are as shown in Table 3.
- Examples 15-17 Example 15 to 17 were the same as Example 1 except that the discharge amounts of the core component polyester and the sheath component polyester were changed to the core: sheath ratio as shown in Table 3. The evaluation results are as shown in Table 3.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Multicomponent Fibers (AREA)
- Knitting Of Fabric (AREA)
- Woven Fabrics (AREA)
Abstract
Description
本発明は、高次工程において毛羽発生が少なく、トリコット用途等、品質品位要求の高い用途においても高次通過性に優れ、熱接着後の織編物が強度、寸法安定性、耐久性に優れ、液体濾過膜の流路材としての品位に優れた熱接着性芯鞘型複合繊維に関するものである。 The present invention has less fuzz generation in high-order processes, is excellent in high-order passage even in applications with high quality requirements such as tricot use, and the woven or knitted fabric after heat bonding is excellent in strength, dimensional stability, and durability. The present invention relates to a heat-adhesive core-sheath composite fiber excellent in quality as a flow passage material for a liquid filtration membrane.
ポリエステル繊維は、その優れた寸法安定性、耐候性、機械的特性、耐久性ならびに比較的安価に大量生産できる生産性等から、衣料、産業資材等の原料繊維として好適であり、様々な分野、用途で使用されている。 Polyester fibers are suitable as raw materials for clothing, industrial materials, etc. due to their excellent dimensional stability, weather resistance, mechanical properties, durability, and productivity that can be mass-produced relatively inexpensively. Used in applications.
近年では、水処理膜の流路材、フィルター等の資材用途、椅子張りやパーテーション等のインテリア用途、その他各種衣料用途などにおいて、ポリエステル繊維を織編物とした後、カレンダー加工等の熱処理を施すことによって、繊維を部分的に溶融させ、繊維同士を熱接着させることで布帛の形態保持性、剛性を向上することのできる熱接着性ポリエステル繊維の利用が進んでいる。中でも、中東・アフリカ地域を中心に人口増加に起因する深刻な水不足の解消に向けて、水処理膜の需要は年々増加しており、水処理装置において濾過された透過水の流路となる部材において、ポリエステルのトリコット編地を熱接着させたポリエステルトリコット流路材の需要が急増している。 In recent years, after using polyester fibers as woven or knitted fabrics, heat treatment such as calendering is applied to water treatment membranes, filter materials, interior materials such as chair upholstery and partitioning, and other clothing applications. Therefore, the use of heat-adhesive polyester fibers that can improve the shape retention and rigidity of the fabric by partially melting the fibers and thermally bonding the fibers to each other is progressing. Above all, the demand for water treatment membranes is increasing year by year in order to eliminate the serious water shortage caused by population growth mainly in the Middle East and Africa. However, the demand for a polyester tricot channel material in which a polyester tricot knitted fabric is thermally bonded is increasing rapidly.
上記熱接着性を有するポリエステル繊維としては、融点または軟化点の異なる2種類以上のポリエステルで構成される糸条が好適である。その態様として、例えば、フィラメント糸からなる混繊糸や、芯鞘型あるいはサイドバイサイド型の複合繊維が挙げられる。融点の異なるフィラメントを単糸レベルで混合した混繊糸に比べ、フィラメント単糸が融点の異なるポリマで構成される複合繊維が熱接着後の品位において優位である。特に、原糸の生産性や熱処理後の布帛の表面平滑性など品位に優れる芯鞘複合糸で、かつ、鞘成分が芯成分よりも融点または軟化点の低い成分で構成される熱接着性芯鞘型複合繊維が、積極的に利用されている。 As the polyester fiber having thermal adhesiveness, a yarn composed of two or more kinds of polyesters having different melting points or softening points is suitable. As the mode, for example, mixed yarn made of filament yarn, core-sheath type or side-by-side type composite fiber can be mentioned. Compared to a mixed yarn in which filaments having different melting points are mixed at the single yarn level, a composite fiber composed of polymers having different melting points is superior in quality after thermal bonding. In particular, a core-sheath composite yarn excellent in quality such as productivity of raw yarn and surface smoothness of the fabric after heat treatment, and the sheath component is composed of a component having a melting point or a softening point lower than that of the core component. Sheath-type composite fibers are actively used.
前記熱接着性芯鞘型複合繊維として、主たる繰り返し単位がエチレンテレフタレートからなるポリエステルを芯部とし、軟化温度が130~200℃であるポリマを鞘部とした芯鞘型複合繊維(特許文献1)が提案されている。 As the heat-adhesive core-sheath type composite fiber, a core-sheath type composite fiber having a polyester whose main repeating unit is ethylene terephthalate as a core part and a polymer having a softening temperature of 130 to 200 ° C. as a sheath part (Patent Document 1) Has been proposed.
上記芯鞘型複合繊維によれば、所定の強伸度特性を有し、熱接着交差点でのズレによる目ずれ、シボが発生せず、品位の良好な熱接着織編物を得ることができるとされる。しかしながら、鞘成分に使用するポリマの好ましい組成として、イソフタル酸を共重合させたポリエステルが例示されているように、鞘部の該ポリマは明確な融点を有さない結晶性の低いものである。このため、該芯鞘型複合繊維からなる織編物は熱接着処理した際に複合繊維同士の接着にムラが生じ、寸法安定性や布帛の強伸度ばらつきなどが生じ、液体濾過膜の流路材として使用した場合の品位に劣るという課題があった。 According to the core-sheath-type conjugate fiber, it has a predetermined strength and elongation characteristic, does not cause misalignment due to displacement at the thermal bonding intersection, and does not generate wrinkles. Is done. However, as a preferred composition of the polymer used for the sheath component, the polymer in the sheath portion has a low crystallinity having no clear melting point, as exemplified by polyester copolymerized with isophthalic acid. For this reason, when the woven or knitted fabric made of the core-sheath type composite fiber is heat-bonded, unevenness occurs in the bonding between the composite fibers, resulting in dimensional stability, variation in the strength and elongation of the fabric, and the like. There was a problem of poor quality when used as a material.
これに対し、繰り返し単位の90モル%以上がエチレンテレフタレートからなるポリマを芯部とし、繰り返し単位の60~90モル%がブチレンテレフタレートからなる共重合ポリブチレンテレフタレートを鞘部とした芯鞘型複合繊維(特許文献2)が提案されている。 On the other hand, a core-sheath type composite fiber in which 90 mol% or more of repeating units have a core made of a polymer composed of ethylene terephthalate and 60 to 90 mol% of repeating units have a copolymer polybutylene terephthalate made of butylene terephthalate as a sheath. (Patent Document 2) has been proposed.
上記芯鞘型複合繊維によれば、鞘成分に適度な結晶性が付与されており、また沸水収縮率、熱収縮応力のピーク温度等の繊維物性が良好であることから、品位の良好な熱接着された織編物製品を得ることができるとされる。 According to the core-sheath type composite fiber, the sheath component is imparted with appropriate crystallinity, and since the fiber physical properties such as the boiling water shrinkage rate and the peak temperature of the heat shrinkage stress are good, the heat of good quality. It is said that a bonded knitted or knitted product can be obtained.
また、特許文献3記載や特許文献4記載の熱接着性芯鞘型複合繊維を使用したトリコット編地も報告されている。これらの技術では、芯成分の高融点ポリエステルに対して、鞘成分の融点が大幅に低いポリエステルを使用しており、芯成分ポリエステルの融点のみから紡糸温度を設定すると、鞘成分の熱劣化が進み易い。一方鞘成分ポリエステルの融点を勘案して紡糸温度を下げると、芯成分の強伸度特性を最大限に発揮できないことから、複合繊維は強伸度に劣る。
In addition, a tricot knitted fabric using the heat-bondable core-sheath composite fiber described in
特許文献2記載の芯鞘型複合繊維は、強伸度に乏しいので、高張力、ハイスピードで加工し、毛羽など原糸の品質欠点が布帛の欠点として顕著に現れるトリコット用途への展開が難しいという問題があった。また、鞘成分の融点が低いことから、織編み後の熱接着温度を高くすることができないため、布帛を構成する複合繊維の収縮が不十分となり、布帛の設計上において高い寸法精度が求められる水処理膜流路材などの用途においては、高圧下で長期間使用した場合の寸法安定性に課題があった。また、特許文献3記載や特許文献4記載の熱接着性芯鞘型複合繊維では、強伸度が劣るため、高次通過性が低いだけでなく、布帛とした時の強伸度が不十分となり、流路材として長期間使用した際の耐久性に劣るといった課題があった。また、特許文献2と同様の理由から、織編み後の熱接着温度を高くすることができないため、布帛を構成する繊維の収縮が不十分となり、布帛の設計で高い寸法精度が求められる水処理膜流路材などの用途において、高圧下で長期間使用した場合の寸法安定性には依然として課題があった。
Since the core-sheath type composite fiber described in Patent Document 2 has poor strength and elongation, it is difficult to develop into a tricot application in which high-tension and high-speed processing is performed, and the quality defect of the raw yarn such as fluff is prominent as a defect of the fabric. There was a problem. Moreover, since the melting point of the sheath component is low, the heat bonding temperature after weaving and knitting cannot be increased, so that the shrinkage of the composite fibers constituting the fabric is insufficient, and high dimensional accuracy is required in designing the fabric. In applications such as a water treatment membrane channel material, there was a problem in dimensional stability when used for a long time under high pressure. In addition, the heat-adhesive core-sheath type composite fibers described in
本発明は、従来技術の課題を解消し、高次工程において毛羽発生が少なく、トリコット用途等、品質品位要求の高い用途においても高次通過性に優れ、熱接着後の織編物が強度、寸法安定性、耐久性に優れ、液体濾過膜の流路材としての品位に優れた熱接着性芯鞘型複合繊維を提供する。 The present invention eliminates the problems of the prior art, has less fuzz generation in high-order processes, is excellent in high-order passage even in applications with high quality requirements such as tricot use, and the woven or knitted fabric after heat bonding has strength, dimensions Provided is a heat-adhesive core-sheath composite fiber that is excellent in stability and durability and excellent in quality as a flow passage material for a liquid filtration membrane.
上記課題を解決するため、本発明は次の構成からなる。
(1)融点250℃以上のポリエステルを芯部に、融点215℃以上、かつ芯部を構成するポリエステルより融点が20~35℃低いポリエステルを鞘部とした芯鞘型複合繊維であって、強度が3.8cN/dtex以上、伸度が35%以上であることを特徴とする熱接着性芯鞘型複合繊維。
(2)芯鞘型複合繊維の総繊度が30dtex以上、単糸繊度が3.0dtex以下である(1)記載の熱接着性芯鞘型複合繊維。
(3)(1)または(2)記載の熱接着性芯鞘型複合繊維を構成に含むトリコット編み地。
In order to solve the above problems, the present invention has the following configuration.
(1) A core-sheath type composite fiber having a polyester having a melting point of 250 ° C. or higher as a core, a melting point of 215 ° C. or higher and a polyester having a melting point 20 to 35 ° C. lower than that of the polyester constituting the core. Is a heat-adhesive core-sheath-type composite fiber, characterized by having a tensile strength of 3.8 cN / dtex or more and an elongation of 35% or more.
(2) The heat-adhesive core-sheath conjugate fiber according to (1), wherein the core-sheath conjugate fiber has a total fineness of 30 dtex or more and a single yarn fineness of 3.0 dtex or less.
(3) A tricot knitted fabric comprising the heat-adhesive core-sheath composite fiber according to (1) or (2) in its configuration.
本発明によれば、高次工程において毛羽発生が少なく、トリコット用途等、品質品位要求の高い用途においても高次通過性に優れ、熱接着後の織編物が強度、寸法安定性、耐久性に優れ、液体濾過膜の流路材としての品位に優れた熱接着性芯鞘型複合繊維を提供することができる。 According to the present invention, there is little fluffing in a high-order process, excellent high-order passability even in applications with high quality requirements such as tricot use, and the woven or knitted fabric after heat bonding has strength, dimensional stability, and durability. It is possible to provide a heat-bondable core-sheath composite fiber that is excellent and excellent in quality as a flow passage material for a liquid filtration membrane.
以下、本発明の熱接着性芯鞘型複合繊維について詳述する。
本発明の芯鞘型複合繊維は、芯成分の融点が250℃以上のポリエステル、鞘成分の融点が215℃以上で、かつ芯部を構成するポリエステルの融点より20~35℃低いポリエステルで構成される。
Hereinafter, the heat-adhesive core-sheath composite fiber of the present invention will be described in detail.
The core-sheath type composite fiber of the present invention is composed of a polyester having a melting point of the core component of 250 ° C. or higher, a polyester having a melting point of 215 ° C. or higher, and 20 to 35 ° C. lower than the melting point of the polyester constituting the core. The
芯成分ポリエステルの融点を250℃以上とすることで、ポリエステルの持つ強伸度特性を最大限に発揮できる程度に紡糸温度を高くすることができ、布帛とした時の強度、耐久性に優れる。芯成分ポリエステルの融点は、実用上の上限から270℃以下であることが好ましい。芯成分ポリエステルの融点が270℃以下であることで、極端に高温紡糸する必要がなく、汎用的な溶融紡糸装置を用いて紡糸できるため好ましい。さらに好ましくは253℃以上、260℃以下である。 By setting the melting point of the core component polyester to 250 ° C. or higher, the spinning temperature can be increased to such an extent that the strength and elongation characteristics of the polyester can be maximized, and the strength and durability when used as a fabric are excellent. The melting point of the core component polyester is preferably 270 ° C. or less from the practical upper limit. It is preferable that the melting point of the core component polyester is 270 ° C. or lower because it is not necessary to perform spinning at an extremely high temperature and spinning can be performed using a general-purpose melt spinning apparatus. More preferably, it is 253 degreeC or more and 260 degrees C or less.
鞘成分ポリエステルの融点は、215℃以上であり、250℃以下であることが好ましい。鞘成分ポリエステルの融点が250℃以下であると、布帛を熱接着する際、汎用的な装置を使用でき、また、熱接着処理における油剤成分に起因する発煙を抑えることができるため好ましい。さらに好ましくは、220℃以上、235℃以下である。鞘成分ポリエステルと芯成分ポリエステルの融点差を20℃以上とすることで、布帛の熱接着温度を芯成分ポリエステルの融点より十分に低い温度とすることができ、原糸の強度を活かした、高耐久の布帛とすることができる。また、融点差を35℃以下とすることで、紡糸温度を芯成分ポリエステルの強伸度を最大限に引き出し、かつ鞘成分ポリエステルの熱劣化を極力抑える温度に設定することができるため、強伸度に優れ、原糸毛羽の少ない品位に優れた複合繊維となる。鞘成分ポリエステルと芯成分ポリエステルの融点差は、好ましくは23℃以上、30℃以下である。 The melting point of the sheath component polyester is 215 ° C or higher, preferably 250 ° C or lower. It is preferable that the melting point of the sheath component polyester is 250 ° C. or lower because a general-purpose apparatus can be used when the fabric is thermally bonded, and fuming caused by the oil component in the thermal bonding treatment can be suppressed. More preferably, it is 220 degreeC or more and 235 degreeC or less. By making the melting point difference between the sheath component polyester and the core component polyester 20 ° C. or more, the thermal bonding temperature of the fabric can be made sufficiently lower than the melting point of the core component polyester, It can be a durable fabric. Further, by setting the difference in melting point to 35 ° C. or less, the spinning temperature can be set to a temperature that maximizes the strength of the core component polyester and suppresses the thermal degradation of the sheath component polyester as much as possible. This is a composite fiber that is superior in quality and excellent in quality with little raw yarn fluff. The difference in melting point between the sheath component polyester and the core component polyester is preferably 23 ° C. or higher and 30 ° C. or lower.
また、芯成分ポリエステルの軟化温度は245℃以上であることが好ましく、鞘成分ポリエステルの軟化温度は205℃以上であることが好ましい。芯成分ポリエステルの軟化温度が245℃以上であることで、鞘成分ポリエステルの融点以上で布帛を熱接着処理した際に、寸法変化が少なく布帛の形態が安定するため好ましい。芯成分ポリエステルの軟化温度は、さらに好ましくは250℃以上である。芯成分ポリエステルの軟化温度の上限温度は実用上270℃である。 Also, the softening temperature of the core component polyester is preferably 245 ° C. or higher, and the softening temperature of the sheath component polyester is preferably 205 ° C. or higher. It is preferable that the softening temperature of the core component polyester is 245 ° C. or higher because when the fabric is heat-bonded at the melting point or higher of the sheath component polyester, the dimensional change is small and the fabric form is stable. The softening temperature of the core component polyester is more preferably 250 ° C. or higher. The upper limit temperature of the softening temperature of the core component polyester is practically 270 ° C.
鞘成分ポリエステルの軟化温度が205℃以上であることで、加工工程における熱セット時のヒーターへの融着がなく、高速通過性が安定するので好ましい。鞘成分ポリエステルの軟化温度は、さらに好ましくは215℃以上である。鞘成分ポリエステルの融点を215℃以上、軟化点を205℃以上とすることで、布帛とした後の熱接着温度を十分に高くすることができるため、熱接着処理によって芯鞘複合繊維の熱収縮が進み、最終製品の寸法安定性が向上するため好ましい。鞘成分ポリエステルの軟化温度の上限温度は実用上250℃である。 It is preferable that the softening temperature of the sheath component polyester is 205 ° C. or higher because there is no fusion to the heater during heat setting in the processing step, and the high-speed passage is stable. The softening temperature of the sheath component polyester is more preferably 215 ° C. or higher. By setting the melting point of the sheath component polyester to 215 ° C. or higher and the softening point to 205 ° C. or higher, the thermal bonding temperature after forming the fabric can be sufficiently increased. Is preferable because the dimensional stability of the final product is improved. The upper limit temperature of the softening temperature of the sheath component polyester is practically 250 ° C.
芯成分ポリエステルとしては、融点が上記範囲内であれば任意のポリエステルを選択できるが、寸法安定性、強伸度特性からポリエチレンテレフタレート(以下、PETと称する)とすることが好ましい。PETとはテレフタル酸を主たる酸成分とし、エチレングリコールを主たるグリコール成分として得られるポリエステルである。芯成分ポリエステルは、融点が前述の範囲内であれば適宜共重合成分を含むものであってもよい。共重合可能な化合物としては、例えばPETに対して、イソフタル酸、コハク酸、シクロヘキサンジカルボン酸、アジピン酸、ダイマ酸、セバシン酸、5-ナトリウムスルホイソフタル酸などのジカルボン酸類、エチレングリコール、ジエチレングリコール、2,2-ジメチル-1,3-プロパンジオール、ブタンジオール、ネオペンチルグリコール、シクロヘキサンジメタノール、ポリエチレングリコール、ポリプロピレングリコール、ビスフェノールAエチレンオキサイド付加物などのジオール類を挙げることができるが、寸法安定性、強伸度特性から、100%がエチレンテレフタレートの繰り返し単位からなるホモPETであることがさらに好ましい。また、必要に応じて、艶消し剤として二酸化チタンなどの無機微粒子、滑剤としてシリカ微粒子などを添加してもよい。 As the core component polyester, any polyester can be selected as long as the melting point is within the above range, but polyethylene terephthalate (hereinafter referred to as PET) is preferable from the viewpoint of dimensional stability and strong elongation characteristics. PET is a polyester obtained using terephthalic acid as the main acid component and ethylene glycol as the main glycol component. The core component polyester may appropriately include a copolymer component as long as the melting point is within the above-described range. Examples of the copolymerizable compound include PET, dicarboxylic acids such as isophthalic acid, succinic acid, cyclohexanedicarboxylic acid, adipic acid, dimer acid, sebacic acid, 5-sodium sulfoisophthalic acid, ethylene glycol, diethylene glycol, 2 , 2-dimethyl-1,3-propanediol, butanediol, neopentyl glycol, cyclohexanedimethanol, polyethylene glycol, polypropylene glycol, bisphenol A ethylene oxide adduct, and the like. From the viewpoint of the strength and elongation characteristics, it is more preferable that the PET is a homo-PET comprising 100% repeating units of ethylene terephthalate. If necessary, inorganic fine particles such as titanium dioxide as a matting agent and silica fine particles as a lubricant may be added.
鞘成分ポリエステルとしては、融点が前述範囲内であれば任意のポリエステルを選択できるが、PETのほか、ポリトリメチレンテレフタレートやポリブチレンテレフタレートが好ましい。芯成分ポリエステルとしてPETを使用する場合、複合界面の剥離抑制を考慮すると、鞘成分ポリエステルとしてPETを使用することが特に好ましい。鞘成分ポリエステルは、融点が前述の範囲内であれば任意の共重合成分を任意の割合で添加することができるが、70モル%以上がエチレンテレフタレートの繰り返し単位からなる共重合PETとすると、ポリマに適度な結晶性を付与することができ、紡糸の操業性が安定するため好ましい。また、布帛を熱接着した際に熱接着ムラが生じにくくなり好ましい。80モル%以上がエチレンテレフタレートの繰り返し単位からなる共重合PETであるとさらに好ましい。鞘成分ポリエステルとしてPET以外のポリマを使用する場合も、原糸生産性や布帛の熱接着処理後の品位を損なわない範囲で、適宜共重合成分を添加可能である。共重合成分としては、前述の共重合成分など任意の成分を共重合することができる。また、選択したポリマ種によらず、必要に応じて、艶消し剤として二酸化チタンなどの無機微粒子、滑剤としてシリカ微粒子などを添加してもよい。 As the sheath component polyester, any polyester can be selected as long as the melting point is within the above-mentioned range, but in addition to PET, polytrimethylene terephthalate and polybutylene terephthalate are preferable. When PET is used as the core component polyester, it is particularly preferable to use PET as the sheath component polyester in consideration of suppression of peeling at the composite interface. As the sheath component polyester, an arbitrary copolymer component can be added at an arbitrary ratio as long as the melting point is within the above-mentioned range. However, when the copolymer PET is composed of 70% by mole or more of ethylene terephthalate repeating units, Moderate crystallinity can be imparted, and spinning operability is stabilized. In addition, when the fabric is thermally bonded, thermal bonding unevenness is less likely to occur, which is preferable. More preferably, 80 mol% or more is a copolymerized PET composed of ethylene terephthalate repeating units. Even when a polymer other than PET is used as the sheath component polyester, a copolymer component can be appropriately added within a range that does not impair the raw yarn productivity and the quality of the fabric after the thermal bonding treatment. As a copolymerization component, arbitrary components, such as the above-mentioned copolymerization component, can be copolymerized. In addition, inorganic fine particles such as titanium dioxide as a matting agent and silica fine particles as a lubricant may be added as needed, regardless of the polymer species selected.
次に複合繊維の固有粘度(以下、IVと称する)は0.55~0.75であることが好ましい。IVが0.55以上であると重合度が低すぎることもなく、複合繊維が実用に耐えるのに十分なタフネスが達成できるので好ましい。一方、IVが0.75以下であれば、紡糸時にIVが高すぎることもなく、極端な高温紡糸をする必要もなく、溶融紡糸中のCOOH量の増大を抑制でき、メルトフラクチャーが生じることもなく、均一な複合繊維が得られ、タフネスを低下させることもないので好ましい。より好ましくはIVは0.60~0.70の範囲である。 Next, the intrinsic viscosity (hereinafter referred to as IV) of the composite fiber is preferably 0.55 to 0.75. When the IV is 0.55 or more, the degree of polymerization is not too low, and it is preferable because the toughness sufficient for the composite fiber to withstand practical use can be achieved. On the other hand, if the IV is 0.75 or less, the IV is not too high at the time of spinning, there is no need to perform extreme high temperature spinning, the increase in the amount of COOH during melt spinning can be suppressed, and melt fracture may occur. This is preferable because a uniform composite fiber is obtained and the toughness is not lowered. More preferably, IV is in the range of 0.60 to 0.70.
図1は本発明の芯鞘型複合繊維の断面模式図であって、芯成分1の周囲を鞘成分2で取り囲んだ芯鞘型複合繊維10である。
FIG. 1 is a schematic cross-sectional view of a core-sheath type composite fiber of the present invention, which shows a core-sheath
複合繊維の断面形状は、高融点成分を芯部に、低融点成分を芯部を覆う鞘型に配置すれば特に限定されるものではないが、鞘成分が芯成分を完全に覆い、芯成分の露出がないと好ましい。また、原糸の生産性やウースター斑U%など物性の安定性のため、複合繊維の断面において、複合繊維全体の重心に対する芯成分の重心の偏心率は5%以下であることが好ましい。偏心率が5%以下であると芯成分と鞘成分のポリマの組み合わせが収縮差の生じる組み合わせであったとしてもコイル状の捲縮が発現せず、布帛品位に優れるため好ましい。さらに好ましくは偏心率は1%以下である。 The cross-sectional shape of the composite fiber is not particularly limited as long as the high melting point component is disposed in the core portion and the low melting point component is disposed in the sheath shape covering the core portion, but the sheath component completely covers the core component, and the core component It is preferable that there is no exposure. In addition, for the stability of physical properties such as the productivity of raw yarn and Uster spots U%, the eccentricity of the center of gravity of the core component with respect to the center of gravity of the entire composite fiber is preferably 5% or less in the cross section of the composite fiber. An eccentricity of 5% or less is preferable because a coil-like crimp does not appear even if the combination of the core component and the sheath component is a combination that causes a shrinkage difference, and the fabric quality is excellent. More preferably, the eccentricity is 1% or less.
また、複合繊維の断面外周形状は、外周形状の長径をA、短径をBとしたときA/Bで表される扁平率が1.1以下の略円形とすることが好ましい。このような形状とすることで、外部張力を受けたときに均一に力を分散して受けることができ、複合繊維のS-Sカーブにおける強伸度バラツキも少なくなり好ましい。さらに好ましくは扁平率は1.0である。 The cross-sectional outer peripheral shape of the composite fiber is preferably a substantially circular shape having a flatness expressed by A / B of 1.1 or less, where A is the major axis and B is the minor axis. By adopting such a shape, it is possible to uniformly receive the force when subjected to external tension, and it is preferable because variations in the strength and elongation of the composite fiber in the SS curve are reduced. More preferably, the aspect ratio is 1.0.
芯鞘型複合繊維における芯成分と鞘成分の複合比率は、断面積比が芯:鞘=40:60~90:10であることが好ましく、更に好ましくは55:45~75:25である。複合比率を上記範囲内とすることで、複合繊維が安定製糸可能で、強伸度に優れるとともに、毛羽発生が少なく、布帛を熱接着した際にも強伸度が維持できるため好ましい。 The composite ratio of the core component to the sheath component in the core-sheath composite fiber is preferably such that the cross-sectional area ratio is core: sheath = 40: 60 to 90:10, and more preferably 55:45 to 75:25. By making the composite ratio within the above range, it is preferable because the composite fiber can be stably spun and excellent in high elongation, less fuzz is generated, and the high elongation can be maintained even when the fabric is thermally bonded.
芯成分に含まれる無機粒子の含有率は3.0重量%以下とすることでタフネスが向上するため好ましく、さらに好ましくは0.5重量%以下である。鞘成分に含まれる無機微粒子の含有率は0.05重量%以上であると工程通過性が向上するため好ましい。より好ましくは鞘成分に含まれる無機微粒子の含有率は0.05重量%以上、0.5重量%以下が工程通過中にガイドを過度に摩耗させることが無く、流路材として使用した際、不要な無機粒子の脱落がなく好ましい。無機微粒子は酸化チタンが複合繊維としての工程通過性の面から好ましい。 The content of the inorganic particles contained in the core component is preferably 3.0% by weight or less because the toughness is improved, and more preferably 0.5% by weight or less. The content of the inorganic fine particles contained in the sheath component is preferably 0.05% by weight or more because process passability is improved. More preferably, the content of the inorganic fine particles contained in the sheath component is 0.05% by weight or more and 0.5% by weight or less without excessive wear of the guide during the process, when used as a flow path material, It is preferable because unnecessary inorganic particles are not dropped off. The inorganic fine particles are preferably titanium oxide from the viewpoint of process passability as a composite fiber.
本発明の複合繊維において、総繊度は30dtex以上が好ましい。総繊度を30dtex以上とすることで、熱接着処理しても十分な強度と剛性を担保することができ、流路材として使用した際は、水圧が作用しても十分な透過液の通水量を確保可能となる。総繊度は、好ましくは90dtex以下であり、さらに好ましくは40dtex以上である。総繊度を90dtex以下とすることで、布帛の薄地化が図れ、流路材として使用した際、濾過膜と流路材の貼り合わせからなる単位あたりの積層数を増やせて好ましい。 In the composite fiber of the present invention, the total fineness is preferably 30 dtex or more. By setting the total fineness to 30 dtex or more, sufficient strength and rigidity can be ensured even by heat bonding treatment, and when used as a flow path material, a sufficient amount of permeate flows even if water pressure acts. Can be secured. The total fineness is preferably 90 dtex or less, more preferably 40 dtex or more. By setting the total fineness to 90 dtex or less, the fabric can be thinned, and when used as a flow path material, the number of layers per unit formed by bonding the filtration membrane and the flow path material can be increased.
また、複合繊維の単糸繊度は3.0dtex以下が好ましい。単糸繊度を3.0dtex以下とすることで、比表面積が大きく、短時間の熱接着処理でも均一に熱接着でき、熱接着処理による布帛の強度低下を抑制することができるため、高耐久な布帛を得ることができる。単糸繊度は、好ましくは0.7dtex以上であり、さらに好ましくは、1.5dtex以上、2.5dtex以下である。単糸繊度を0.7dtex以上とすることで、糸ムラや原糸毛羽が少なく、安定的に製糸可能であり、また、編成糸切れが少なく高次通過性に優れ、布帛とした際にも適度な剛性が得られるため好ましい。 The single yarn fineness of the composite fiber is preferably 3.0 dtex or less. By setting the single yarn fineness to 3.0 dtex or less, the specific surface area is large, it can be uniformly heat-bonded even in a short-time heat bonding treatment, and the fabric strength can be prevented from being lowered by the heat bonding treatment. A fabric can be obtained. The single yarn fineness is preferably 0.7 dtex or more, and more preferably 1.5 dtex or more and 2.5 dtex or less. By setting the single yarn fineness to 0.7 dtex or more, there is little yarn unevenness and raw yarn fluff, and stable yarn production is possible. It is preferable because an appropriate rigidity can be obtained.
複合繊維の強度は3.8cN/dtex以上、伸度は35%以上である。強度を3.8cN/dtex以上とすることで、布帛にした際にその強力が高く、流路材として使用した際の耐久性に優れる。実用上の上限は強度7.0cN/dtexである。また、伸度を35%以上とすることで、原糸の毛羽が防止でき、さらには織編み時の整経毛羽、編成時の糸切れが少なく高次通過性に優れるとともに、欠点の少ない品位に優れた布帛となる。伸度は35~50%であることがさらに好ましい。伸度を50%以下とすることで得られる織編物が寸法安定性に優れるため好ましい。 The strength of the composite fiber is 3.8 cN / dtex or more, and the elongation is 35% or more. By setting the strength to 3.8 cN / dtex or more, the strength is high when used as a fabric, and the durability when used as a flow path material is excellent. The practical upper limit is a strength of 7.0 cN / dtex. Moreover, by setting the elongation to 35% or more, it is possible to prevent the fluff of the original yarn, and further, the warp fluff at the time of weaving and knitting, the yarn breakage at the time of knitting is excellent, and the high-passability is excellent, and there are few defects. It becomes an excellent fabric. More preferably, the elongation is 35 to 50%. A woven or knitted fabric obtained by setting the elongation to 50% or less is preferable because of excellent dimensional stability.
複合繊維の繊維長手方向の太さムラの指標であるウースター斑U%は、均一性の高い布帛を得るために1.4%以下とすることが好ましい。ウースター斑U%1.4%以下であると熱接着後の布帛表面が平滑となり、流路材として使用した際、均一な流路を形成できるので好ましい。より好ましくはウースター斑U%1.0%以下である。 In order to obtain a highly uniform fabric, it is preferable that the Worcester unevenness U%, which is an index of thickness unevenness in the fiber longitudinal direction of the composite fiber, is 1.4% or less. Wooster spots U% of 1.4% or less is preferable because the surface of the fabric after thermal bonding becomes smooth and a uniform channel can be formed when used as a channel material. More preferably, the Wooster plaque U% is 1.0% or less.
複合繊維の乾熱収縮率は20%以下であることが好ましい。乾熱収縮率20%以下とすることで、熱接着処理による寸法変化を抑えることができるため好ましい。実用上の下限は乾熱収縮率2.0%である。 The dry heat shrinkage of the composite fiber is preferably 20% or less. It is preferable to set the dry heat shrinkage rate to 20% or less because dimensional changes due to thermal bonding treatment can be suppressed. The practical lower limit is a dry heat shrinkage of 2.0%.
本発明の目的を達成するための好ましい製糸方法を説明する。
本発明の熱接着性芯鞘型複合繊維の溶融紡糸方法に用いる口金は、既存の複合紡糸用口金を用いることができる。
A preferred yarn production method for achieving the object of the present invention will be described.
As the die used for the melt spinning method of the heat-adhesive core-sheath composite fiber of the present invention, an existing composite spinning die can be used.
溶融方法は、プレッシャーメルターによる方法、エクストルーダーによる方法が挙げられるが、エクストルーダーによる溶融が効率と分解抑制の観点から好ましい。溶融温度は使用するポリマの融点よりも10~40℃高温に設定することが好ましい。 Examples of the melting method include a method using a pressure melter and a method using an extruder, but melting using an extruder is preferable from the viewpoint of efficiency and suppression of decomposition. The melting temperature is preferably set to 10 to 40 ° C. higher than the melting point of the polymer used.
好ましい紡糸温度は280~295℃である。さらに好ましくは紡糸温度は285℃~293℃である。このような紡糸温度を採用することにより、高タフネスで製糸性の良好な複合繊維を得ることができる。口金直下での急冷を緩和するため、口金下に加熱ヒーターを設けてもよい。 A preferable spinning temperature is 280 to 295 ° C. More preferably, the spinning temperature is 285 ° C to 293 ° C. By adopting such a spinning temperature, it is possible to obtain a composite fiber having high toughness and good spinning properties. In order to mitigate the rapid cooling immediately below the base, a heater may be provided under the base.
溶融から吐出までの溶融通過時間、加熱時間は極力短くすることで、芯成分、鞘成分それぞれの分子量低下を抑制することができるため好ましい。芯成分、鞘成分は、ともに別々に溶融混練され、加熱ゾーンを経て精密に吐出計量し、異物補足の濾過層を通過して、芯鞘型となるよう複合口金を用いて吐出・糸条化・冷却される。この溶融から吐出までの通過時間であるポリマ滞留時間は、30分以内であると、ポリマの熱劣化を軽減でき、IV低下が押さえられ、糸のタフネス低下を防止することができる。また複合繊維中のCOOH量の増加を抑制できるため、毛羽が抑制され、耐熱性に優れるとともに、高次通過性に優れ、布帛としたときの耐久性が向上できるので好ましい。より好ましくはポリマ滞留時間20分以下である。 It is preferable to shorten the melt passage time and the heating time from melting to discharge as much as possible because the molecular weight reduction of the core component and the sheath component can be suppressed. Both the core component and sheath component are melted and kneaded separately, precisely discharged and weighed through a heating zone, passed through a filtration layer supplemented with foreign matter, and discharged and formed into a core and sheath using a composite die.・ Cooled. When the polymer residence time, which is the transit time from melting to ejection, is within 30 minutes, thermal degradation of the polymer can be reduced, IV reduction can be suppressed, and yarn toughness reduction can be prevented. Moreover, since the increase in the amount of COOH in the composite fiber can be suppressed, fluff is suppressed, heat resistance is excellent, high-order passage property is excellent, and durability when used as a fabric can be improved, which is preferable. More preferably, the polymer residence time is 20 minutes or less.
強伸度と生産性のバランスから、口金面温度は270℃以上、290℃以下とすることが好ましい。口金面温度は270℃以上とすることで、芯成分の特性を最大限に引き出すことができ、強伸度に優れた糸条を得ることができる。口金面温度を290℃以下とすることで、口金直下でのポリマ加水分解物の堆積による糸切れ増加が抑制され、原糸生産性に優れるので好ましい。 From the balance between strong elongation and productivity, the die surface temperature is preferably 270 ° C. or higher and 290 ° C. or lower. By setting the base surface temperature to 270 ° C. or higher, the core component characteristics can be maximized, and a yarn excellent in high elongation can be obtained. By setting the die surface temperature to 290 ° C. or less, an increase in yarn breakage due to deposition of polymer hydrolyzate directly under the die is suppressed, and this is preferable because it is excellent in raw yarn productivity.
本発明の芯鞘型複合繊維は、吐出されたポリマを未延伸糸として一旦巻き取った後に延伸する2工程法のほか、紡糸および延伸工程を連続して行う直接紡糸延伸法や高速製糸法などの1工程法、いずれのプロセスにおいても製造できる。 The core-sheath type composite fiber of the present invention is not only a two-step method in which the discharged polymer is once wound up as an undrawn yarn and then drawn, as well as a direct spinning drawing method or a high-speed spinning method in which spinning and drawing steps are continuously performed. It can be produced by any one-step method.
延伸温度としては、未延伸糸のガラス転移温度付近である60℃以上、100℃以下で行なうことが好ましい。延伸温度を60℃以上とすることで均一延伸でき、100℃以下とすることで延伸ロールへの融着や繊維の自発伸長による生産性悪化を防ぐことができる。さらに好ましくは延伸温度は75℃以上、95℃以下である。 The stretching temperature is preferably 60 ° C. or higher and 100 ° C. or lower, which is near the glass transition temperature of the undrawn yarn. Uniform stretching can be achieved by setting the stretching temperature to 60 ° C. or higher, and productivity deterioration due to fusion to a stretching roll or spontaneous elongation of fibers can be prevented by setting the stretching temperature to 100 ° C. or lower. More preferably, the stretching temperature is 75 ° C. or higher and 95 ° C. or lower.
また、延伸後には、未延伸糸の結晶速度が最大となる温度で熱セットすることが好ましく、110℃以上、180℃以下とすることが好ましい。110℃以上で熱セットすることで繊維の結晶化を促進し、強度を高くすることができるだけでなく、収縮応力、乾熱収縮率を始め、各種の糸物性の安定化が図れるので好ましい。また、180℃以下で熱セットすることで、熱セット装置への複合繊維の融着による生産性悪化を防ぐことができるため好ましい。 In addition, after drawing, it is preferable to heat-set at a temperature at which the crystal speed of the undrawn yarn is maximized, and it is preferably set to 110 ° C. or higher and 180 ° C. or lower. Heat setting at 110 ° C. or higher is preferable because it can not only promote fiber crystallization and increase strength, but also stabilize various yarn properties such as shrinkage stress and dry heat shrinkage. Moreover, it is preferable to heat-set at 180 ° C. or lower because productivity deterioration due to fusion of the composite fiber to the heat-setting device can be prevented.
以下、実施例を挙げて具体的に説明する。なお、実施例の主な測定値は以下の方法で測定した。 Hereinafter, specific examples will be described. In addition, the main measured value of the Example was measured with the following method.
(1)固有粘度(IV)
定義式のηrは、純度98%以上のO-クロロフェノール(OCP)10mL中に試料を0.8g溶かし、25℃の温度にてオストワルド粘度計を用いて相対粘度ηrを下記の式により求め、固有粘度(IV)を算出した。
ηr=η/η0=(t×d)/(t0×d0)
固有粘度(IV)=0.0242ηr+0.2634
[η:ポリマ溶液の粘度、η0:OCPの粘度、t:溶液の落下時間(秒)、d:溶液の密度(g/cm3)、t0:OCPの落下時間(秒)、d0:OCPの密度(g/cm3)] 。
(1) Intrinsic viscosity (IV)
Ηr of the definition formula is obtained by dissolving 0.8 g of a sample in 10 mL of O-chlorophenol (OCP) having a purity of 98% or more, and obtaining the relative viscosity ηr using an Ostwald viscometer at a temperature of 25 ° C. according to the following formula: Intrinsic viscosity (IV) was calculated.
ηr = η / η0 = (t × d) / (t0 × d0)
Intrinsic viscosity (IV) = 0.0242 ηr + 0.2634
[Η: viscosity of polymer solution, η0: OCP viscosity, t: solution drop time (second), d: solution density (g / cm 3 ), t0: OCP drop time (second), d0: OCP Density (g / cm 3 )].
(2)融点
TA Instruments社製示差走査熱量測定(DSC)Q100を用いて、乾燥した試料を10mg秤量し、アルミパンに封入後、窒素雰囲気下で室温から300℃まで昇温速度16℃/分にて測定した。1回目の測定(1st run)後、5分間保持した後室温まで急冷し、連続して2回目の測定(2nd run)を実施し、2nd runにおいてその融解ピークのピークトップ温度を融点とした。
(2) Melting point Using a differential scanning calorimetry (DSC) Q100 manufactured by TA Instruments, 10 mg of the dried sample was weighed, sealed in an aluminum pan, and heated from room temperature to 300 ° C. under a nitrogen atmosphere at a rate of temperature increase of 16 ° C./min. Measured with After the first measurement (1st run), the sample was held for 5 minutes and then rapidly cooled to room temperature. The second measurement (2nd run) was continuously performed, and the peak top temperature of the melting peak in 2nd run was taken as the melting point.
(3)軟化温度
セイコーインスツルメンツ社製熱的機械的装置(TMA/SS-6000)を用いて、乾燥した試料を試料台に設置し、先端径1.0mmの針入プローブを使用して、測定荷重10g、窒素雰囲気下で室温から300℃まで昇温速度16℃/分にて測定した。変位開始時の温度を軟化温度とした。
(3) Softening temperature Using a thermal mechanical device (TMA / SS-6000) manufactured by Seiko Instruments Inc., place the dried sample on the sample stage and measure using a needle probe with a tip diameter of 1.0 mm. Measurement was performed at a temperature increase rate of 16 ° C./min from room temperature to 300 ° C. under a load of 10 g and a nitrogen atmosphere. The temperature at the start of displacement was defined as the softening temperature.
(4)断面偏心率
繊維の断面をキーエンス(株)社マイクロスコープVHX-2000を用いて観察し、付属の画像解析ソフトにて各値を測定し、芯成分の重心位置をC1(図2の3)、複合繊維の重心位置をCf(図2の4)とし、複合繊維の半径をrf(図2の5)としたとき、以下の式から断面偏心率を算出した。
断面偏心率(%)={|Cf-C1|/rf}×100 。
(4) Cross-section eccentricity The cross-section of the fiber was observed using a Keyence Corporation microscope VHX-2000, each value was measured with the attached image analysis software, and the center-of-gravity position of the core component was determined as C1 (see FIG. 2). 3) When the center of gravity of the composite fiber is Cf (4 in FIG. 2) and the radius of the composite fiber is rf (5 in FIG. 2), the cross-sectional eccentricity is calculated from the following equation.
Cross-section eccentricity (%) = {| Cf−C1 | / rf} × 100.
(5)断面扁平率
(4)と同様の方法で、複合繊維断面を観察し、断面の中心を通る径の中で最長を長径A、最短を短径Bとし、以下の式にしたがって断面扁平率を算出した。
断面扁平率 = 長径A/短径B 。
(5) Cross-sectional flatness In the same manner as in (4), the cross-section of the composite fiber is observed, and the longest is the longest diameter A and the shortest is the shortest diameter B among the diameters passing through the center of the cross section. The rate was calculated.
Cross-sectional flatness = major axis A / minor axis B
(6)繊度、強度、伸度、タフネス
JIS L1013(2010、化学繊維フィラメント糸試験方法)に従い測定した。タフネスは以下の式にて算出した。
(タフネス)=(強度)×(伸度)0.5 。
(6) Fineness, strength, elongation, toughness Measured according to JIS L1013 (2010, chemical fiber filament yarn test method). The toughness was calculated by the following formula.
(Toughness) = (Strength) × (Elongation) 0.5
(7)ウースター斑U%
Zellweger社製USTER TESTER 4-CXを使用し、200m/分の速度で5分間糸を給糸しながらノーマルモードで測定を行った。
(7) Wooster spots U%
Measurement was performed in the normal mode while feeding the yarn at a speed of 200 m / min for 5 minutes using a Zellerweger USTER TESTER 4-CX.
(8)沸水収縮率、乾熱収縮率
枠周1.0mの検尺機を用いて10回分のカセを作製し、以下の式に従い計算した。なお、原長、処理後長ともに測定時は荷重{(表示繊度(dtex)×2)g}をかけて測定した。収縮処理について、沸水収縮率は沸騰水中に15分間浸漬、乾熱収縮率は200℃で5分間処理した。
収縮率(%)={(原長(L1)-処理後長(L2))/原長(L1)}×100 。
(8) Boiling water shrinkage rate, dry heat shrinkage rate Using a measuring machine with a frame circumference of 1.0 m, 10 casses were prepared and calculated according to the following formula. Incidentally, both the original length and the length after treatment were measured by applying a load {(display fineness (dtex) × 2) g}. Regarding the shrinkage treatment, the boiling water shrinkage was immersed in boiling water for 15 minutes, and the dry heat shrinkage was treated at 200 ° C. for 5 minutes.
Shrinkage rate (%) = {(original length (L1) −post-treatment length (L2)) / original length (L1)} × 100.
(9)毛羽欠点数
東レエンジニアリング(株)製フライカウンター(MFC-120S)を用いて、解舒速度=500m/分、測定長=50000mの測定条件で、複合繊維48本を測定し、検出された毛羽個数をカウントした。カウントされた毛羽個数に基づき、以下の点数とした。
3点:全48本が0個
2点:48本の平均個数が0.1個未満、かつ48本中の最大個数が1個
1点:48本の平均個数が0.1個以上0.3個未満、かつ48本中の最大個数が1個
0点:48本の平均個数が0.3個以上または、48本中の最大個数が2個以上 。
(9) The number of fluff defects Using a fly counter (MFC-120S) manufactured by Toray Engineering Co., Ltd., 48 composite fibers were measured and detected under the measurement conditions of unwinding speed = 500 m / min and measurement length = 50000 m. The number of fluff was counted. Based on the counted number of fluff, the following points were obtained.
3 points: all 48 are 0 2 points: the average number of 48 is less than 0.1, and the maximum number of 48 is 1 1 point: the average number of 48 is 0.1 or more. Less than 3 and the maximum number of 48 is 1 0 point: The average number of 48 is 0.3 or more, or the maximum number of 48 is 2 or more.
(10)高次通過性
本発明の複合繊維を整経後、フロント糸、バック糸ともに本発明により得られた原糸を使用して、2枚筬からなるトリコット編機(36ゲージ)を用いてダブルデンビー組織の閉じ目で編成した際の、整経毛羽検知個数、編成糸切れ回数に応じ、以下の評価点数とした。
3点:整経毛羽0.3個/千万m未満、かつ編成糸切れ0.5回/200m未満
2点:整経毛羽0.3個/千万m以上0.6個/千万m未満かつ編成糸切れ0.5回/200m未満、または、整経毛羽0.3個/千万m未満かつ編成糸切れ0.5回/200m以上1.0回/200m未満
1点:整経毛羽0.3個/千万m以上0.6個/千万m未満かつ編成糸切れ0.5回/200m以上1.0回/200m未満
0点:整経毛羽0.6個/千万m以上、または編成糸切れ1.0回/200m以上 。
(10) High-passability After warping the conjugate fiber of the present invention, using the yarn obtained by the present invention for both the front yarn and the back yarn, using a tricot knitting machine (36 gauge) consisting of two sheets Thus, the following evaluation points were used according to the number of warp fluff detected and the number of knitting yarn breaks when knitting with a closed double denby structure.
3 points: warp fluff 0.3 pieces / less than 10 million m and knitting yarn breakage 0.5 times / less than 200 m 2 points: warp fluff 0.3 pieces / ten million m or more 0.6 pieces / 10 million m Less than knitting yarn break 0.5 times / 200 m, or warping fluff 0.3 pieces / less than 10 million m and knitting yarn breakage 0.5 times / 200 m or more and less than 1.0 times / 200
(11)熱接着後の布帛の強度
(10)の方法でトリコット編み地を作製し、無荷重状態でピンテンター乾燥機にて、鞘成分の融点+10℃による熱処理を実施し、熱接着された布帛を作製した。熱接着後の布帛の密度はウェール方向が66本/2.54cm(=インチ)、コース方向が53本/2.54cm(=インチ)になるように調整した。熱接着後の布帛強度をウェール(タテ)、コース(ヨコ)方向それぞれにおいて、JIS 1096:2010(織物及び編物の生地試験方法)に準じて測定し、強度値に基づいて下記点数とした。
3点:タテ600N/5cm以上かつヨコ100N/5cm以上
2点:タテ500N/5cm以上600N/5cm未満かつヨコ100N/5cm以上、またはタテ600N/5cm以上かつヨコ80N/5cm以上100N/5cm未満
1点:タテ500N/5cm以上600N/5cm未満かつヨコ80N/5cm以上100N/5cm未満
0点:タテ500N/5cm未満またはヨコ80N/5cm未満 。
(11) Strength of fabric after thermal bonding A tricot knitted fabric is prepared by the method of (10), heat-treated at a melting point of the sheath component + 10 ° C. in a pin tenter dryer under no load, and thermally bonded. Was made. The density of the fabric after heat bonding was adjusted so that the wale direction was 66 / 2.54 cm (= inch) and the course direction was 53 / 2.54 cm (= inch). The fabric strength after heat bonding was measured according to JIS 1096: 2010 (fabric and knitted fabric test method) in each of the wale (vertical) and course (horizontal) directions, and the following scores were obtained based on the strength values.
3 points: vertical 600 N / 5 cm or more and horizontal 100 N / 5 cm or more 2 points: vertical 500 N / 5 cm or more and less than 600 N / 5 cm and horizontal 100 N / 5 cm or more, or vertical 600 N / 5 cm or more and horizontal 80 N / 5 cm or more 100 N / 5
(12)流路材耐水試験(塩の除去率(%)、造水量(m3/日))
(11)と同様に作製した熱接着後のトリコット編み地を、厚さ150μmのRO分離膜2枚の間に挟みスパイラル型ユニットを形成し、直径が0.2m、長さ1mのモジュールに組み込み、TDS(溶解性蒸発残留物)が3.5重量%の海水を液温25℃で4.5MPaの差圧を与えて5日間ろ過した。5日間経過後に透過液の電気伝導度を測定し、硫酸マグネシウム塩の除去率を算出した。また5日経過後の透過液量を測定し、一日あたりの造水量を算出した。試験の結果を踏まえて、以下の評価点数とした。
3点:硫酸マグネシウム塩の除去率が99.8%以上かつ造水量が45m3/日以上
2点:硫酸マグネシウム塩の除去率が99.8%以上かつ造水量が40m3/日以上45m3/日未満、または、硫酸マグネシウム塩の除去率が99.0%以上99.8%未満かつ造水量が45m3/日以上
1点:硫酸マグネシウム塩の除去率が99.0%以上99.8%未満かつ造水量が40m3/日以上45m3/日未満
0点:硫酸マグネシウム塩の除去率が99.0%未満、または造水量が40m3/日未満 。
(12) Channel material water resistance test (salt removal rate (%), water production (m 3 / day))
A tricot knitted fabric after heat bonding produced in the same manner as in (11) is sandwiched between two 150 μm thick RO separation membranes to form a spiral unit, and incorporated into a module having a diameter of 0.2 m and a length of 1 m. Then, seawater having a TDS (soluble evaporation residue) of 3.5% by weight was filtered at a liquid temperature of 25 ° C. with a differential pressure of 4.5 MPa for 5 days. After 5 days, the electric conductivity of the permeate was measured, and the removal rate of the magnesium sulfate salt was calculated. Further, the amount of permeated liquid after 5 days was measured, and the amount of fresh water produced per day was calculated. Based on the results of the test, the following evaluation points were used.
3 points: Magnesium sulfate salt removal rate of 99.8% or more and water production amount of 45 m 3 / day or more 2 points: Magnesium sulfate salt removal rate of 99.8% or more and water production amount of 40 m 3 / day or more of 45 m 3 / Day or the removal rate of magnesium sulfate salt is 99.0% or more and less than 99.8% and the amount of water produced is 45 m 3 / day or more 1 point: The removal rate of magnesium sulfate salt is 99.0% or more and 99.8% %, And the amount of water produced is 40 m 3 / day or more and less than 45 m 3 / day 0 point: The removal rate of magnesium sulfate salt is less than 99.0%, or the amount of water produced is less than 40 m 3 / day.
(13)合否判定
(9)~(12)の評価項目において、全てが2点以上である場合を合格とし、一つでも1点以下である場合を不合格とした。
(13) Pass / Fail Judgment In the evaluation items (9) to (12), a case where all were 2 or more points was accepted, and a case where even one was 1 point or less was rejected.
実施例1
酸化チタンを含有しないIV0.67のホモPETポリマ(高融点成分、融点255℃)と、共重合成分としてイソフタル酸およびビスフェノールAエチレンオキサイド付加物を全酸成分に対してそれぞれ7.1モル%、4.4モル%共重合した、酸化チタン含有率が0.05wt%、IV0.65の共重合PETポリマ(低融点成分、融点230℃)を準備し、高融点成分はエクストルーダーにて285℃にて溶融し、低融点成分はエクストルーダーにて260℃にて溶融し、紡糸温度を290℃に設定し、計量ポンプによる計量を行い、パック内での濾過を経て、口金ノズルにて図1のような同心円芯鞘断面形状(断面偏心率が0%、断面扁平率が1.0)となるように複合面積比率65:35の芯鞘複合型に吐出させた。このとき、高融点成分が芯に、低融点成分が鞘となるように配置した。
Example 1
A homo-PET polymer of IV0.67 containing no titanium oxide (high melting point component, melting point 255 ° C.) and isophthalic acid and bisphenol A ethylene oxide adduct as the copolymer component are each 7.1 mol% based on the total acid component, A copolymerized PET polymer (low melting point component, melting point 230 ° C.) having a titanium oxide content of 0.05 wt% and IV 0.65 copolymerized with 4.4 mol% was prepared, and the high melting point component was 285 ° C. with an extruder. The low melting point component was melted at 260 ° C with an extruder, the spinning temperature was set at 290 ° C, weighed with a metering pump, filtered in a pack, and then with a nozzle nozzle as shown in FIG. It was discharged into a core-sheath composite type having a composite area ratio of 65:35 so that the cross-sectional shape of the concentric circular core-sheath was as follows (the cross-sectional eccentricity was 0% and the cross-sectional flatness was 1.0). At this time, it arrange | positioned so that a high melting component may become a core and a low melting component may become a sheath.
引取装置としては、延伸、巻取りまで一貫して行う直接紡糸法(DSD)を採用し、吐出したポリマは冷却部、給油部を経て、1728m/分の速度、85℃の表面温度に設定された引取りロール(第1HR)にて引き取り、一旦巻き取ることなく、連続して4489m/分、128℃に設定された熱処理ロール(第2HR)に引き回し、2.6倍の延伸を実施した。延伸、熱処理された糸条はそれぞれ4549m/分、4584m/分の速度に設定されたゴデットローラ(第3GR、第4GR)にて張力調整し、4500m/分の速度で0.20cN/dtexの張力にてチーズ状パッケージを巻き取り、56dtex-24フィラメントの芯鞘型複合繊維を得た。得られた繊維に対する評価結果を表1に示した。ウースター斑U%は0.4%、沸水収縮率は10.3%、乾熱収縮率は17.2%であった。 As the take-up device, a direct spinning method (DSD) is used which is consistently performed from drawing to winding, and the discharged polymer is set at a speed of 1728 m / min and a surface temperature of 85 ° C. through the cooling part and the oiling part. Then, the film was taken up by a take-up roll (first HR) and continuously drawn up to a heat treatment roll (second HR) set to 128 ° C. at 4489 m / min without being wound up, and stretched 2.6 times. The tension of the stretched and heat-treated yarns is adjusted with godet rollers (3rd GR and 4GR) set to speeds of 4549 m / min and 4584 m / min, respectively, and the tension is 0.20 cN / dtex at a speed of 4500 m / min. The cheese-like package was wound up to obtain a core-sheath type composite fiber of 56 dtex-24 filaments. The evaluation results for the obtained fibers are shown in Table 1. The Wooster spot U% was 0.4%, the boiling water shrinkage was 10.3%, and the dry heat shrinkage was 17.2%.
表1に示したように、強伸度、タフネスに優れ、原糸毛羽の発生が少なく良好であった。得られた原糸をフロント糸、バック糸双方に使用して、2枚筬からなるトリコット編機(36ゲージ)を用いてダブルデンビー組織の閉じ目で編成したところ、整経毛羽発生、編成切れが少なく高次通過性に優れていた。さらに240℃(鞘成分の融点+10℃)ピンテンターによる熱接着処理後の布帛強度が高く、水処理膜の流路材として使用したところ、高温熱処理を実施したことに起因してトリコット流路材は寸法安定性に優れ、連続使用における流路材の破損や目詰まりなどもなく、膜性能を維持したまま安定した造水量を確保できた。 As shown in Table 1, it was excellent in high elongation and toughness, and it was good with little generation of raw yarn fluff. The resulting yarn was used for both the front yarn and the back yarn, and was knitted with a double denby structure using a tricot knitting machine (36 gauge) consisting of two pieces of warp. There were few, and it was excellent in high-order passage property. Furthermore, the fabric strength after heat bonding with a pin tenter at 240 ° C. (melting point of sheath component + 10 ° C.) is high, and when used as a channel material for a water treatment membrane, Excellent dimensional stability, and there was no damage or clogging of the channel material during continuous use, and a stable amount of fresh water could be secured while maintaining membrane performance.
実施例2~4、比較例1~3
実施例2~4、比較例1~3は芯成分ポリエステル、鞘成分ポリエステルの融点を、それぞれ実施例1の鞘成分で使用した共重合成分を用いて共重合比率を変更し、表1の通りの融点に調整し、それにともなってそれぞれ適切な紡糸温度を採用した以外は実施例1に準じた。評価結果は表1の通りである。
Examples 2 to 4 and Comparative Examples 1 to 3
In Examples 2 to 4 and Comparative Examples 1 to 3, the melting points of the core component polyester and the sheath component polyester were changed using the copolymer components used in the sheath component of Example 1, respectively. In accordance with Example 1, except that an appropriate spinning temperature was adopted. The evaluation results are shown in Table 1.
実施例5
実施例5は、紡糸機をDSDから2工程法に変更し、付随して紡糸条件等を調整した以外は実施例1に準じた。評価結果は表1の通りである。
Example 5
Example 5 was the same as Example 1 except that the spinning machine was changed from DSD to the two-step method and the spinning conditions were adjusted accordingly. The evaluation results are shown in Table 1.
実施例6~7
実施例6~7は口金の吐出孔形状を変更し、断面形状と芯鞘の偏心率を表2の通り変更した以外は実施例1に準じた。評価結果は表2の通りである。
Examples 6-7
Examples 6 to 7 were the same as Example 1 except that the shape of the discharge hole of the base was changed and the cross-sectional shape and the eccentricity of the core sheath were changed as shown in Table 2. The evaluation results are shown in Table 2.
実施例8~11
実施例8~11は複合繊維の繊度、フィラメント数を表2の通り変更した以外は実施例1に準じた。評価結果は表2の通りである。
Examples 8-11
Examples 8 to 11 were the same as Example 1 except that the fineness of the composite fiber and the number of filaments were changed as shown in Table 2. The evaluation results are shown in Table 2.
実施例12~14
実施例12~14は芯成分ポリエステル、鞘成分ポリエステルに添加する酸化チタン量を表3の通り変更した以外は、実施例1に準じた。評価結果は表3の通りである。
Examples 12-14
Examples 12 to 14 were the same as Example 1 except that the amount of titanium oxide added to the core component polyester and the sheath component polyester was changed as shown in Table 3. The evaluation results are as shown in Table 3.
実施例15~17
実施例15~17は芯成分ポリエステル、鞘成分ポリエステルの吐出量を変更し、表3の通りの芯:鞘比率とした以外は実施例1に準じた。評価結果は表3の通りである。
Examples 15-17
Examples 15 to 17 were the same as Example 1 except that the discharge amounts of the core component polyester and the sheath component polyester were changed to the core: sheath ratio as shown in Table 3. The evaluation results are as shown in Table 3.
1 芯成分
2 鞘成分
3 芯成分の重心位置
4 複合繊維の重心位置
5 複合繊維の半径
10 熱接着性芯鞘複合繊維
DESCRIPTION OF
Claims (3)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16/481,928 US20200040484A1 (en) | 2017-02-09 | 2018-02-06 | Thermally adhesive sheath-core conjugate fiber and tricot fabric |
| CN201880010784.2A CN110268109B (en) | 2017-02-09 | 2018-02-06 | Heat-adhesive core-sheath composite fibers and warp knitted fabrics |
| JP2018513569A JP6610778B2 (en) | 2017-02-09 | 2018-02-06 | Heat-adhesive core-sheath composite fiber and tricot knitted fabric |
| KR1020197017284A KR102502868B1 (en) | 2017-02-09 | 2018-02-06 | Heat-sealed core-sheath type composite fiber and tricot letter |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2017022048 | 2017-02-09 | ||
| JP2017-022048 | 2017-02-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2018147251A1 true WO2018147251A1 (en) | 2018-08-16 |
Family
ID=63107478
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2018/003927 Ceased WO2018147251A1 (en) | 2017-02-09 | 2018-02-06 | Thermally adhesive sheath-core conjugate fiber and tricot fabric |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20200040484A1 (en) |
| JP (1) | JP6610778B2 (en) |
| KR (1) | KR102502868B1 (en) |
| CN (1) | CN110268109B (en) |
| WO (1) | WO2018147251A1 (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2020058999A (en) * | 2018-10-12 | 2020-04-16 | 株式会社クボタ | Membrane element and membrane separation equipment |
| JP2020062598A (en) * | 2018-10-17 | 2020-04-23 | 株式会社クボタ | Membrane element, membrane separation equipment and membrane element manufacturing method |
| KR102172280B1 (en) * | 2019-05-13 | 2020-10-30 | 도레이첨단소재 주식회사 | Thermal adhesive polyester composition, thermal adhesive polyester complex-fiber comprising the same, and non-woven fabric |
| WO2022030280A1 (en) * | 2020-08-05 | 2022-02-10 | 東レ株式会社 | Protective garment and method for producing same |
| KR20240046863A (en) | 2021-08-26 | 2024-04-11 | 도레이 카부시키가이샤 | Spunbond nonwoven fabric and separator containing it |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102102040B1 (en) | 2018-07-31 | 2020-04-17 | 도레이첨단소재 주식회사 | Fouling resistant reverse osmosis membrane, manufacturing method thereof and fouling resistant reverse osmosis module containing the same |
| KR102235399B1 (en) | 2019-09-17 | 2021-04-01 | 도레이첨단소재 주식회사 | Filter structure having optional both ends collecting function and Filtering mehod using the same |
| KR102816001B1 (en) | 2019-09-18 | 2025-05-30 | 도레이첨단소재 주식회사 | reverse osmosis membrane and manufacturing method thereof |
| KR102172284B1 (en) | 2019-10-29 | 2020-10-30 | 도레이첨단소재 주식회사 | Spiral wound type membrane module and manufacturing methof thereof |
| KR102347498B1 (en) * | 2020-04-17 | 2022-01-05 | 도레이첨단소재 주식회사 | Spiral membrane module with low elution of heavy metal and preparing method of the same |
| CN115182087A (en) * | 2021-04-07 | 2022-10-14 | 江苏福斯得纺织有限公司 | Processing technology of high-waterproofness textile fabric |
| KR102534675B1 (en) * | 2021-04-09 | 2023-05-18 | 도레이첨단소재 주식회사 | Thermally adhesive composite fiber with excellent elastic rebound and fiber assemblies comprising the same |
| CN113151962A (en) * | 2021-05-17 | 2021-07-23 | 嵊州盛泰针织有限公司 | Novel anti-pilling sandwich knitted fabric and production process thereof |
| KR102642537B1 (en) * | 2021-08-17 | 2024-02-28 | 도레이첨단소재 주식회사 | Antimony non elution tricot fabric filtration and Manufaturing method thereof |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH08302527A (en) * | 1995-05-02 | 1996-11-19 | Unitika Ltd | Heat-adhesive conjugate continuous fiber yarn and sheet |
| JP2000119918A (en) * | 1998-10-12 | 2000-04-25 | Mitsubishi Rayon Co Ltd | Heat-adhesive polyester core-sheath composite fiber and method for producing the same |
| JP2005023436A (en) * | 2003-06-30 | 2005-01-27 | Toray Ind Inc | Special fiber |
| JP2006138046A (en) * | 2004-11-15 | 2006-06-01 | Toray Ind Inc | Spunbonded nonwoven fabric for heat sealing and filter produced by using the same |
| JP2009131840A (en) * | 2007-11-05 | 2009-06-18 | Toray Ind Inc | Separation membrane support, and separation membrane and fluid separation element using the same |
| JP2011001663A (en) * | 2009-06-22 | 2011-01-06 | Toray Ind Inc | Conjugated fiber |
| JP2011245454A (en) * | 2010-05-28 | 2011-12-08 | Fukui Tateami Kogyo Kk | Tricot knitted fabric for flow passage material to be used in liquid separation apparatus and method for producing the fabric |
| WO2012008617A1 (en) * | 2010-07-14 | 2012-01-19 | セーレン株式会社 | Fibrous fabric and manufacturing method for same |
| WO2017114313A1 (en) * | 2015-12-28 | 2017-07-06 | 东丽纤维研究所(中国)有限公司 | Core-sheath type composite fibre, false-twist yarns and fibrous structure |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62184119A (en) | 1986-02-03 | 1987-08-12 | Teijin Ltd | Heat bonding fiber |
| JP3313878B2 (en) * | 1994-03-16 | 2002-08-12 | 日本エステル株式会社 | Polyester binder fiber |
| JPH11241228A (en) * | 1998-02-26 | 1999-09-07 | Nippon Ester Co Ltd | Polyester-based heat-bonding fiber and cushion structure |
| JP3559475B2 (en) * | 1999-06-15 | 2004-09-02 | 日東電工株式会社 | Liquid separation membrane module |
| JP3924217B2 (en) * | 2002-07-30 | 2007-06-06 | ユニチカ株式会社 | Molded carpet |
| WO2008032379A1 (en) * | 2006-09-14 | 2008-03-20 | Toray Industries, Inc. | Polyester fiber, woven knit fabric, car sheet and process for producing polyester fiber |
| JP5019991B2 (en) * | 2007-07-30 | 2012-09-05 | ユニチカ株式会社 | Method for producing spunlace composite nonwoven fabric |
| KR20090047894A (en) * | 2007-11-08 | 2009-05-13 | 주식회사 코오롱 | Spunbond nonwoven fabric for drain board filter material and its manufacturing method |
| CN102162152B (en) * | 2010-02-21 | 2013-07-17 | 东丽纤维研究所(中国)有限公司 | Polyester fiber and fabric |
| KR20130035414A (en) * | 2011-09-30 | 2013-04-09 | 코오롱인더스트리 주식회사 | Polyester nonwoven fabric and method for manufacturing the same |
| JP5917944B2 (en) * | 2012-02-23 | 2016-05-18 | 日東電工株式会社 | Blended nonwoven fabric, filter media and filter unit |
| JP5943797B2 (en) | 2012-09-27 | 2016-07-05 | ユニチカトレーディング株式会社 | Warp knitted fabric |
-
2018
- 2018-02-06 CN CN201880010784.2A patent/CN110268109B/en active Active
- 2018-02-06 US US16/481,928 patent/US20200040484A1/en not_active Abandoned
- 2018-02-06 JP JP2018513569A patent/JP6610778B2/en active Active
- 2018-02-06 KR KR1020197017284A patent/KR102502868B1/en active Active
- 2018-02-06 WO PCT/JP2018/003927 patent/WO2018147251A1/en not_active Ceased
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH08302527A (en) * | 1995-05-02 | 1996-11-19 | Unitika Ltd | Heat-adhesive conjugate continuous fiber yarn and sheet |
| JP2000119918A (en) * | 1998-10-12 | 2000-04-25 | Mitsubishi Rayon Co Ltd | Heat-adhesive polyester core-sheath composite fiber and method for producing the same |
| JP2005023436A (en) * | 2003-06-30 | 2005-01-27 | Toray Ind Inc | Special fiber |
| JP2006138046A (en) * | 2004-11-15 | 2006-06-01 | Toray Ind Inc | Spunbonded nonwoven fabric for heat sealing and filter produced by using the same |
| JP2009131840A (en) * | 2007-11-05 | 2009-06-18 | Toray Ind Inc | Separation membrane support, and separation membrane and fluid separation element using the same |
| JP2011001663A (en) * | 2009-06-22 | 2011-01-06 | Toray Ind Inc | Conjugated fiber |
| JP2011245454A (en) * | 2010-05-28 | 2011-12-08 | Fukui Tateami Kogyo Kk | Tricot knitted fabric for flow passage material to be used in liquid separation apparatus and method for producing the fabric |
| WO2012008617A1 (en) * | 2010-07-14 | 2012-01-19 | セーレン株式会社 | Fibrous fabric and manufacturing method for same |
| WO2017114313A1 (en) * | 2015-12-28 | 2017-07-06 | 东丽纤维研究所(中国)有限公司 | Core-sheath type composite fibre, false-twist yarns and fibrous structure |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2020058999A (en) * | 2018-10-12 | 2020-04-16 | 株式会社クボタ | Membrane element and membrane separation equipment |
| JP7228360B2 (en) | 2018-10-12 | 2023-02-24 | 株式会社クボタ | Membrane elements and membrane separation equipment |
| JP2020062598A (en) * | 2018-10-17 | 2020-04-23 | 株式会社クボタ | Membrane element, membrane separation equipment and membrane element manufacturing method |
| JP7228361B2 (en) | 2018-10-17 | 2023-02-24 | 株式会社クボタ | MEMBRANE ELEMENT MANUFACTURING METHOD |
| KR102172280B1 (en) * | 2019-05-13 | 2020-10-30 | 도레이첨단소재 주식회사 | Thermal adhesive polyester composition, thermal adhesive polyester complex-fiber comprising the same, and non-woven fabric |
| WO2020231166A1 (en) * | 2019-05-13 | 2020-11-19 | 도레이첨단소재 주식회사 | Polyester composition for thermally adhesive fiber, thermally adhesive composite fiber implemented therethrough, and nonwoven fabric |
| WO2022030280A1 (en) * | 2020-08-05 | 2022-02-10 | 東レ株式会社 | Protective garment and method for producing same |
| KR20240046863A (en) | 2021-08-26 | 2024-04-11 | 도레이 카부시키가이샤 | Spunbond nonwoven fabric and separator containing it |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20190107658A (en) | 2019-09-20 |
| KR102502868B1 (en) | 2023-02-23 |
| JP6610778B2 (en) | 2019-11-27 |
| CN110268109B (en) | 2022-07-22 |
| JPWO2018147251A1 (en) | 2019-06-27 |
| US20200040484A1 (en) | 2020-02-06 |
| CN110268109A (en) | 2019-09-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP6610778B2 (en) | Heat-adhesive core-sheath composite fiber and tricot knitted fabric | |
| KR101412284B1 (en) | Liquid crystalline polyester fiber and process for production of the same | |
| CN102165110B (en) | Polyester monofilament, method for producing same, and method for producing screen gauze using same | |
| JP5286827B2 (en) | Liquid crystal polyester fiber | |
| JP5098693B2 (en) | Liquid crystal polyester fiber | |
| TW567257B (en) | Polytrimethyleneterephthalate modified cross section yarn | |
| WO2016052269A1 (en) | Polyester filament package | |
| JP4325387B2 (en) | Polyester monofilament for screen bag and method for producing the same | |
| JP5187224B2 (en) | Method for producing molten liquid crystalline polyester fiber | |
| JP5862076B2 (en) | Polyester monofilament for screens | |
| JP2005248357A (en) | Polyester monofilament for screen gauze | |
| JP3753658B2 (en) | Polytrimethylene terephthalate multifilament yarn | |
| JP7176413B2 (en) | High tenacity fine polyester multifilament | |
| JP2005047020A (en) | Polyester monofilament for screen gauze | |
| CN116490649B (en) | Sea-island composite polyester fiber | |
| JP7304285B2 (en) | Mesh fabric made of liquid crystal polyester fiber | |
| JP2009242952A (en) | Polyester multifilament, method for producing the same, and base fabric for adhesive layer | |
| JP2012211399A (en) | Polyester monofilament | |
| JP2022113213A (en) | Polyester-based composite mixed fiber processed yarn | |
| JP2020193411A (en) | Polyester multifilament | |
| JP2008163492A (en) | Polyester monofilament for screens | |
| JPH06166908A (en) | Ultrafine fiber and its production | |
| JP2009256822A (en) | Monofilament for screen gauze |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ENP | Entry into the national phase |
Ref document number: 2018513569 Country of ref document: JP Kind code of ref document: A |
|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 18751435 Country of ref document: EP Kind code of ref document: A1 |
|
| ENP | Entry into the national phase |
Ref document number: 20197017284 Country of ref document: KR Kind code of ref document: A |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 18751435 Country of ref document: EP Kind code of ref document: A1 |